Canonical Allele Identifier: CA658653863

Gene: TCN2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.30615613_30615614dup , CM000684.2:g.30615613_30615614dup	GRCh38
NC_000022.10:g.31011600_31011601dup , CM000684.1:g.31011600_31011601dup	GRCh37
NC_000022.9:g.29341600_29341601dup	NCBI36
NG_007263.1:g.13440_13441dup , LRG_116:g.13440_13441dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471659.2:n.2243_2244dup
ENST00000698263.1:c.766_767dup	ENSP00000513635.1:p.Met258ProfsTer?
ENST00000698264.1:n.2243_2244dup
ENST00000698265.1:c.766_767dup	ENSP00000513636.1:p.Met258ProfsTer?
ENST00000698266.1:c.766_767dup	ENSP00000513637.1:p.Met258ProfsTer?
ENST00000698267.1:c.766_767dup	ENSP00000513638.1:p.Met258ProfsTer?
ENST00000698268.1:c.766_767dup	ENSP00000513639.1:p.Met258ProfsTer?
ENST00000698269.1:c.*332_*333dup	ENSP00000513640.1:n.*332_*333dup
ENST00000698270.1:c.613_614dup	ENSP00000513641.1:p.Met207ProfsTer?
ENST00000698271.1:c.796_797dup	ENSP00000513642.1:p.Met268ProfsTer?
ENST00000698272.1:c.757_758dup	ENSP00000513643.1:p.Met255ProfsTer?
ENST00000698273.1:c.757_758dup	ENSP00000513644.1:p.Met255ProfsTer?
ENST00000215838.8:c.766_767dup MANE Select	ENSP00000215838.3:p.Met258ProfsTer?
ENST00000215838.7:c.766_767dup	ENSP00000215838.3:p.Met258ProfsTer?
ENST00000405742.7:c.754_755dup	ENSP00000385914.3:p.Met254ProfsTer?
ENST00000407817.3:c.685_686dup	ENSP00000384914.3:p.Met231ProfsTer?
ENST00000450638.5:c.691_692dup	ENSP00000394184.2:p.Met233ProfsTer?
NM_000355.3:c.766_767dup	NP_000346.2:p.Met258ProfsTer?
NM_001184726.1:c.685_686dup	NP_001171655.1:p.Met231ProfsTer?
NM_000355.4:c.766_767dup MANE Select	NP_000346.2:p.Met258ProfsTer?
NM_001184726.2:c.685_686dup	NP_001171655.1:p.Met231ProfsTer?